Who We Are
The Lewy Body Dementia Association (LBDA) is a 501(c)(3) organization and is the leading resource in the United States for those affected by Lewy body dementia (LBD). LBDA is dedicated to providing outreach and education to families struggling with LBD, raising awareness of Lewy body dementia among the general public and medical profession, and advocating for increased research funding.
Through education and outreach we support those affected by Lewy body dementias, and promote research for a cure.
We envision a cure for Lewy body dementias and quality support for those still living with the disease.
What is Lewy Body Dementia?
Afflicting approximately one in every 199 people in the United States, Lewy body dementias (LBD) are a collection of related brain disorders. The common ties between these disorders are the presence of “Lewy bodies” (abnormal protein deposits) in the brain and varying combinations of certain cognitive, motor and psychiatric symptoms.
Join with us today!
Join with the LBDA Volunteer Team! Our Volunteer Team is made up of volunteers throughout the country who give their time and expertise to help support the fight against Lewy body dementias. LBD affects one in 199 people in the United States which means that 1.5 million people living with LBD need your help! As an LBDA Volunteer you can facilitate a support group, provide a one-on-one connection with someone seeking help and information, distribute educational materials within your own community and much more. Many LBDA Volunteer opportunities are virtual and require only that you have access to telephone and internet service. To join the LBDA Volunteer Team click on an opportunity to learn more.
Who We Are
The Lewy Body Dementia Association (LBDA) is a 501(c)(3) organization and is the leading resource in the United States for those affected by Lewy body dementia (LBD). LBDA is dedicated to providing outreach and education to families…